Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs9275572 | 0.724 | 0.360 | 6 | 32711222 | upstream gene variant | A/G;T | snv | 15 | |||
rs6457617 | 0.763 | 0.480 | 6 | 32696074 | intergenic variant | C/A;T | snv | 11 | |||
rs615672 | 0.851 | 0.240 | 6 | 32606394 | intergenic variant | G/A;C | snv | 6 | |||
rs9268856 | 0.807 | 0.240 | 6 | 32461942 | intron variant | C/A;T | snv | 6 | |||
rs3806156 | 0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv | 5 | |||
rs9268645 | 0.827 | 0.360 | 6 | 32440750 | intron variant | C/G;T | snv | 5 | |||
rs9268877 | 0.827 | 0.200 | 6 | 32463370 | intron variant | A/G;T | snv | 5 | |||
rs539703 | 0.882 | 0.200 | 6 | 32320685 | intron variant | A/C;T | snv | 4 | |||
rs10995245 | 0.882 | 0.160 | 10 | 62631615 | intron variant | G/A;C | snv | 3 | |||
rs16830359 | 1.000 | 0.080 | 1 | 43130713 | intergenic variant | G/A;T | snv | 3 | |||
rs3101942 | 0.882 | 0.200 | 6 | 32902280 | intergenic variant | G/A;C | snv | 3 | |||
rs3130311 | 0.882 | 0.200 | 6 | 32249590 | intergenic variant | A/G;T | snv | 3 | |||
rs3134926 | 0.882 | 0.200 | 6 | 32232370 | intergenic variant | C/A;G | snv | 3 | |||
rs455674 | 0.882 | 0.120 | 6 | 39768626 | regulatory region variant | C/G;T | snv | 3 | |||
rs6670122 | 0.882 | 0.120 | 1 | 156737983 | intron variant | T/C;G | snv | 0.99 | 3 | ||
rs9267954 | 0.882 | 0.200 | 6 | 32245275 | regulatory region variant | A/C;T | snv | 3 | |||
rs9268560 | 0.882 | 0.200 | 6 | 32421735 | intergenic variant | C/G;T | snv | 3 | |||
rs11210604 | 0.925 | 0.080 | 1 | 42158001 | downstream gene variant | T/A;G | snv | 2 | |||
rs1154155 | 0.925 | 0.080 | 14 | 22533736 | upstream gene variant | G/A;T | snv | 2 | |||
rs172137 | 0.925 | 0.120 | 5 | 167604857 | intron variant | G/A;T | snv | 2 | |||
rs2305795 | 0.925 | 0.080 | 19 | 10115376 | intron variant | G/A;C | snv | 2 | |||
rs7746922 | 0.925 | 0.200 | 6 | 32463198 | intron variant | C/A;G;T | snv | 2 | |||
rs9272723 | 0.925 | 0.200 | 6 | 32641650 | intron variant | T/C | snv | 2 | |||
rs9274477 | 0.925 | 0.080 | 6 | 32665936 | intron variant | A/G | snv | 2 |